Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Synthesis of bis-quaternary centers at the α-positions of cyclohexanones via Copper(I)-Catalyzed Claisen rearrangement: The substituent effect from the opposing α-quaternary center on diastereoselectivity

Tetrahedron(2024)10.1016/j.tet.2024.134415Source: DataRank Database

Synthesis of bis-quaternary centers at the α-positions of cyclohexanones via Copper(I)-Catalyzed Claisen rearrangement: The substituent effect from the opposing α-quaternary center on diastereoselectivity is a research paper published in Tetrahedron (2024). On theSindex it has a DataRank of 0.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access0 citations

Download PDF

Cite:

Linked data & code

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (2 grants)Impact (FWCI 0.00)OA: greenTopics (21)Linked Datasets (9)DataCite Reuse (9)IDs (PubMed, PMC, OpenAlex)

FAIR Checklist

Context only (not used in score)

Findable (2/2)

Has DOI
Indexed in repositories

Accessible (1/2)

Open Access

Interoperable (2/2)

DataCite relations
Linked datasets

Reusable (0/3)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (7)

Joshua A. Malone,Estefania Armendariz-Gonzalez,A. Muhammad Afdhal Saputra ORCID,Jacob R. Stepherson,Frank R. Fronczek ORCID

Live enrichment

PubMed:39897454 PMC:PMC11784635 OpenAlex:https://openalex.org/W4405311931

National Science Foundation

Grant: HRD-0832999

National Institute of General Medical Sciences

Grant: R01GM127649

FWCI

0.00

Citation Percentile

0.1%

greenLicense: http://www.elsevier.com/open-access/userlicense/1.0/

journalhttps://repository.lsu.edu/chemistry_pubs/3918

repositoryhttps://repository.lsu.edu/chemistry_pubs/3918

publisherhttps://api.elsevier.com/content/article/PII:S0040402024005969?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0040402024005969?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.tet.2024.134415

Fields of Study

Asymmetric Synthesis and CatalysisSynthetic Organic Chemistry MethodsChemical Synthesis and Analysis

Keywords

ChemistryQuaternary carbonClaisen rearrangementSubstituentQuaternaryCopperCarroll rearrangementCatalysisCenter (category theory)StereochemistryMedicinal chemistryOrganic chemistryCrystallographyEnantioselective synthesisStereoselectivityCarbonyl CompoundsCopper CatalysisAllyloxy Allyl Cation

CCDC 2405596: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc2lr6wgCambridge Crystallographic Data Centre

CCDC 2405595: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc2lr6vfCambridge Crystallographic Data Centre

CCDC 2405594: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc2lr6tdCambridge Crystallographic Data Centre

CCDC 2072246: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc27kbntCambridge Crystallographic Data Centre

CCDC 2072245: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc27kbmsCambridge Crystallographic Data Centre

CCDC 2072244: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc27kblrCambridge Crystallographic Data Centre

CCDC 2072243: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc27kbkqCambridge Crystallographic Data Centre

CCDC 2072233: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc27kb7dCambridge Crystallographic Data Centre

CCDC 2072242: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc27kbjpCambridge Crystallographic Data Centre